ReviewChemPlusChem2026
Recent Exploration of Right-Handed D-Sulfonyl-γ-AApeptides as Potential Tools Toward α-Helical Mimicry.
Review in ChemPlusChem, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
2 authors.
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Abstract
Over the last 15 years, our laboratory has explored peptidomimetics in diverse research areas, including AApeptide folding, structure-based design, combinatorial screening, and supramolecular chemistry. Through these efforts, we successfully introduced a new subclass of AApeptides known as sulfonyl-γ-AApeptides. In recent years, we took advantage of the synthetic scaffold and rationally designed and developed helices targeting a series of protein-protein interactions. This Perspective summarizes our recent advances in developing right-handed helical D-sulfonyl-γ-AApeptides, which closely resemble the secondary structure of canonical α-helices and represent a promising platform for α-helical mimicry.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.